Chakrabarty et al., 2018 - Google Patents
Visible light mediated desilylative C (sp 2)–C (sp 2) cross-coupling reactions of arylsilanes with aryldiazonium salts under Au (i)/Au (iii) catalysisChakrabarty et al., 2018
- Document ID
- 13979094589496465086
- Author
- Chakrabarty I
- Akram M
- Biswas S
- Patil N
- Publication year
- Publication venue
- Chemical Communications
External Links
Snippet
Visible light mediated desilylative C(sp 2 )–C(sp 2 ) cross-coupling reactions of arylsilanes
with aryldiazonium salts under Au( i )/Au( iii ) catalys ... - Chemical Communications (RSC
Publishing) DOI:10.1039/C8CC03925A Royal Society of Chemistry View PDF VersionPrevious …
- 239000011780 sodium chloride 0 title abstract description 20
Classifications
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F15/00—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System
- C07F15/0006—Compounds containing elements of Groups 8, 9, 10 or 18 of the Periodic System compounds of the platinum group
- C07F15/0073—Rhodium compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F17/00—Metallocenes
- C07F17/02—Metallocenes of metals of Groups 8, 9 or 10 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07B—GENERAL METHODS OF ORGANIC CHEMISTRY; APPARATUS THEREFOR
- C07B37/00—Reactions without formation or introduction of functional groups containing hetero atoms, involving either the formation of a carbon-to-carbon bond between two carbon atoms not directly linked already or the disconnection of two directly linked carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C45/00—Preparation of compounds having >C = O groups bound only to carbon or hydrogen atoms; Preparation of chelates of such compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F9/00—Compounds containing elements of Groups 5 or 15 of the Periodic System
- C07F9/02—Phosphorus compounds
- C07F9/547—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom
- C07F9/6564—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms
- C07F9/6568—Heterocyclic compounds, e.g. containing phosphorus as a ring hetero atom having phosphorus atoms, with or without nitrogen, oxygen, sulfur, selenium or tellurium atoms, as ring hetero atoms having phosphorus atoms as the only ring hetero atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F7/00—Compounds containing elements of Groups 4 or 14 of the Periodic System
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07F—ACYCLIC, CARBOCYCLIC OR HETEROCYCLIC COMPOUNDS CONTAINING ELEMENTS OTHER THAN CARBON, HYDROGEN, HALOGEN, OXYGEN, NITROGEN, SULFUR, SELENIUM OR TELLURIUM
- C07F5/00—Compounds containing elements of Groups 3 or 13 of the Periodic System
- C07F5/02—Boron compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C201/00—Preparation of esters of nitric or nitrous acid or of compounds containing nitro or nitroso groups bound to a carbon skeleton
- C07C201/06—Preparation of nitro compounds
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07C—ACYCLIC OR CARBOCYCLIC COMPOUNDS
- C07C2/00—Preparation of hydrocarbons from hydrocarbons containing a smaller number of carbon atoms
-
- C—CHEMISTRY; METALLURGY
- C07—ORGANIC CHEMISTRY
- C07D—HETEROCYCLIC COMPOUNDS
- C07D213/00—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members
- C07D213/02—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members
- C07D213/04—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom
- C07D213/06—Heterocyclic compounds containing six-membered rings, not condensed with other rings, with one nitrogen atom as the only ring hetero atom and three or more double bonds between ring members or between ring members and non-ring members having three double bonds between ring members or between ring members and non-ring members having no bond between the ring nitrogen atom and a non-ring member or having only hydrogen or carbon atoms directly attached to the ring nitrogen atom containing only hydrogen and carbon atoms in addition to the ring nitrogen atom
Similar Documents
Publication | Publication Date | Title |
---|---|---|
Chakrabarty et al. | Visible light mediated desilylative C (sp 2)–C (sp 2) cross-coupling reactions of arylsilanes with aryldiazonium salts under Au (i)/Au (iii) catalysis | |
Cornilleau et al. | Gold-catalysed cross-coupling between aryldiazonium salts and arylboronic acids: probing the usefulness of photoredox conditions | |
Maksymowicz et al. | Catalytic asymmetric carbon–carbon bond formation using alkenes as alkylmetal equivalents | |
Fulmer et al. | Solvent-free Sonogashira coupling reaction via high speed ball milling | |
Makida et al. | Nickel-catalysed carboxylation of organoboronates | |
Akram et al. | Gold (I)-catalyzed cross-coupling reactions of aryldiazonium salts with organostannanes | |
Li et al. | Benzimidazolium‐Pyrazole‐Palladium (II) Complexes: New and Efficient Catalysts for Suzuki, Heck and Sonogashira Reactions | |
Huynh et al. | Pincer-type di (1, 2, 4-triazolin-5-ylidene) Pd (II) complexes and their catalytic activities towards Cu-and amine-free Sonogashira reaction | |
Agrawal et al. | Observation of Binuclear Palladium Clusters upon ESI-MS Monitoring of the Suzuki–Miyaura Cross-Coupling Catalyzed by a Dichloro-bis (aminophosphine) Complex of Palladium | |
Smirnov et al. | Photoredox generation of the trifluoromethyl radical from borate complexes via single electron reduction | |
Guzmán et al. | Ir-catalyzed selective reduction of CO 2 to the methoxy or formate level with HSiMe (OSiMe 3) 2 | |
Mu et al. | Fast Suzuki–Miyaura cross-coupling reaction catalyzed by the Na2Pd2Cl6 complex with ethyl calix [4] aryl acetate at room temperature in aqueous medium under ligand-free and ambient atmosphere | |
Amadio et al. | A new palladium (II)–allyl complex containing a thioether-triazole ligand as active catalyst in Suzuki–Miyaura reaction. Use of tetraalkylammonium salts as promoters: Influence of the salt anion and cation on the catalytic activity | |
Harris et al. | Kinetics and Mechanism of the Gold-Catalyzed Intermolecular Hydroalkoxylation of Allenes with Alcohols | |
Maji et al. | Ferrocenyl palladacycles derived from unsymmetrical pincer-type ligands: evidence of Pd (0) nanoparticle generation during the Suzuki–Miyaura reaction and applications in the direct arylation of thiazoles and isoxazoles | |
Noveski et al. | C–F Activation and hydrodefluorination of fluorinated alkenes at rhodium | |
Kumar et al. | Sterically hindered selenoether ligands: Palladium (II) complexes as catalytic activators for Suzuki–Miyaura coupling | |
Liu et al. | Light induced catalytic hydrodefluorination of perfluoroarenes by porphyrin rhodium | |
Dong et al. | A Convenient and Efficient Rhenium‐Catalyzed Hydrosilylation of Ketones and Aldehydes | |
Khaibulova et al. | Steric effect of substituents in haloarenes on the rate of cross-coupling reactions | |
Wolf et al. | Aryl Grignard cross-coupling of aryl chlorides catalysed by new, highly active phosphine/imidazolium nickel (II) complexes | |
Matsheku et al. | Synthesis of new adamantyl-imine palladium (II) complexes and their application in Mizoroki-Heck and Suzuki-Miyaura CC cross-coupling reactions | |
CN104098607A (en) | Complex and application of monophosphine monoazacyclo-carben nickel containing tricyclic hexyl phosphine | |
John et al. | Highly efficient palladium precatalysts of homoscorpionate bispyrazolyl ligands for the more challenging Suzuki–Miyaura cross-coupling of aryl chlorides | |
Hanhan et al. | Microwave-assisted aqueous Suzuki coupling reactions catalyzed by ionic palladium (II) complexes |